Successfully pass audits and inspections instead of causing quality bureaucracy

Most companies find quality management audits and FDA inspections stressful. Our regulatory affairs experts and lead auditors will help you to quickly

  • pass these audits (ISO 13485, ISO 9001) and inspections (21 CFR part 820),
  • establish concise and customized quality management systems (QM systems),
  • streamline your existing QM system, and
  • achieve regulatory compliance fast, with minimum efforts and without having to read hundreds of regulatory documents

Precise and streamlined processes will help not only to achieving regulatory compliance but also to developing high quality products in time and budget.

Create QM-Systems (ISO 13485)

Our auditors and QM experts have assisted literally hundreds of medical device companies to pass audits and inspections successfully (100% success rate)

Mock Audits & Inspections of QM-Systems

Avoid uncertainty or even fear of audits and inspections. Our ISO 13485 lead auditors perform a Mockup audit and perfectly prepare you for the next audit and inspection

External Quality Management Representative

You do not have to do everything yourself: We will gladly support you as an external QM representative.

How Verity Compliance helps

Read more about how we can help to

  • establishing your quality management (QM) system
  • challenging your QM systems with mock-up audits and preparing them for the next audit and inspection
  • overcoming the shortage of personnel e.g. by acting as your external quality representatives.

Contact us now and learn how we can help to develop and maintain your quality management system!